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PMID: 15193306 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

The evolving roles of alternative splicing.

Current opinion in structural biology ·Vol. 14 ·No. 3 ·2004-06-00 ·Pages 273-82

Lareau LF, Green RE, Bhatnagar RS, Brenner SE

Abstract

Alternative splicing is now commonly thought to affect more than half of all human genes. Recent studies have investigated not only the scope but also the biological impact of alternative splicing on a large scale, revealing that its role in generating proteome diversity may be augmented by a role in regulation. For instance, protein function can be regulated by the removal of interaction or localization domains by alternative splicing. Alternative splicing can also regulate gene expression by splicing transcripts into unproductive mRNAs targeted for degradation. To fully understand the scope of alternative splicing, we must also determine how many of the predicted splice variants represent functional forms. Comparisons of alternative splicing between human and mouse genes show that predominant splice variants are usually conserved, but rare variants are less commonly shared. Evolutionary conservation of splicing patterns suggests functional importance and provides insight into the evolutionary history of alternative splicing.

MeSH Terms
Alternative Splicing Animals Apoptosis/genetics Evolution, Molecular Gene Expression Regulation Genetic Techniques Humans Mice Protein Biosynthesis Untranslated Regions
Chemicals
Untranslated Regions
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lareau Liana F
Department of Molecular and Cell Biology, University of California, Berkeley, California 94720, USA.
Green Richard E
Bhatnagar Rajiv S
Brenner Steven E
Article Info
Journal
Current opinion in structural biology
Abbr.
Curr Opin Struct Biol
ISSN
0959-440X
Published
2004-06-00
Pages
273-82
Language
English
Region
England
NLM ID
9107784
Subset
IM
Grants
NHGRI NIH HHS · K22 HG00056 · United States
NIGMS NIH HHS · T32 GM07127 · United States
NHGRI NIH HHS · T32 HG00047 · United States
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